US4906274A - Organic stabilizers - Google Patents

Organic stabilizers Download PDF

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Publication number
US4906274A
US4906274A US07/118,366 US11836687A US4906274A US 4906274 A US4906274 A US 4906274A US 11836687 A US11836687 A US 11836687A US 4906274 A US4906274 A US 4906274A
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United States
Prior art keywords
isothiazolone
alkyl
parts
orthoester
aryl
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
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US07/118,366
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English (en)
Inventor
John R. Mattox
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Rohm and Haas Co
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Rohm and Haas Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Rohm and Haas Co filed Critical Rohm and Haas Co
Priority to US07/118,366 priority Critical patent/US4906274A/en
Priority to CA000580959A priority patent/CA1301061C/en
Priority to IE331088A priority patent/IE62806B1/en
Priority to NO884873A priority patent/NO174991C/no
Priority to MYPI88001255A priority patent/MY103633A/en
Priority to HU885697A priority patent/HU202053B/hu
Priority to MX13658A priority patent/MX164009B/es
Priority to IL88292A priority patent/IL88292A/xx
Priority to AT88310390T priority patent/ATE85053T1/de
Priority to FI885110A priority patent/FI89855C/fi
Priority to BR888805762A priority patent/BR8805762A/pt
Priority to AU24718/88A priority patent/AU609204B2/en
Priority to DE8888310390T priority patent/DE3877899T2/de
Priority to JP63279203A priority patent/JPH0818932B2/ja
Priority to ES88310390T priority patent/ES2053763T3/es
Priority to EP88310390A priority patent/EP0315464B1/de
Priority to DK618388A priority patent/DK618388A/da
Priority to NZ226846A priority patent/NZ226846A/xx
Priority to KR1019880014594A priority patent/KR970007930B1/ko
Priority to PH37825A priority patent/PH24910A/en
Assigned to ROHM AND HAAS COMPANY reassignment ROHM AND HAAS COMPANY ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: MATTOX, JOHN R.
Application granted granted Critical
Publication of US4906274A publication Critical patent/US4906274A/en
Priority to GR920403281T priority patent/GR3006903T3/el
Priority to SG300/93A priority patent/SG30093G/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D275/00Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
    • C07D275/02Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings
    • C07D275/03Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/22Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients stabilising the active ingredients
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/80Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/02Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
    • A01N47/06Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing —O—CO—O— groups; Thio analogues thereof

Definitions

  • This invention relates to stable compositions of 3-isothiazolones, their preparation, and their use in controlling living organisms.
  • the isothiazolones which are stabilized include those disclosed in U.S. Pat. Nos. 3,523,121 and 3,761,488 as represented by the following structural formula ##STR1## wherein Y is an unsubstituted or substituted alkyl of from 1 to 18 carbon atoms, an unsubstituted or halo substituted alkenyl or alkynyl of from 2 to 8 carbon atoms, and, preferably, from 2 to 4 carbon atoms, an unsubstituted or substituted cycloalkyl of from 5 to 8 carbon atoms, an unsubstituted or substituted aralkyl or an unsubstituted or substituted aryl;
  • R is hydrogen, halo, or a (C 1 -C 4 )alkyl and R 1 is hydrogen, halo or (C 1 -C 4 )alkyl.
  • Y substituents include methyl, ethyl, propyl, isopropyl, butyl, hexyl, octyl, cyclohexyl, benzyl, 3,4-dichlorobenzyl, 4-methoxybenzyl, 4-chlorobenzyl, 3,4-dichlorophenyl, 4-methoxyphenyl, hydroxymethyl, chloromethyl, chloropropyl and the like.
  • Preferred isothiazolones are 5-chloro-2-methyl-3-isothiazolone, 2-methyl-3-isothiazolone, 2-octyl-3-isothiazolone, 4,5-dichloro-2-cyclohexyl-3-isothiazolone and 4,5-dichloro-2-octyl-3-isothiazolone.
  • Japanese Pat. No. 12243183 discloses stabilizing a mixture of an isothiazolone and 2-hydroxymethyl-2-nitro-1,3-propanediol with a diol solvent.
  • 2-hydroxymethyl-2-nitro-1,3-propanediol is a formaldehyde releaser, which is known to stabilize isothiazolones (see U.S. Pat. Nos. 4,165,318 and 4,129,448).
  • European Patent Application 194,146 discloses stabilizing isothiazolones in non-aqueous, salt-free systems by several hydroxylic solvents, outstanding among them dipropylene glycol.
  • Formaldehyde is a suspected carcinogen, and it is desirable not to use formaldehyde in applications where contact with human skin or lungs may occur.
  • This invention is directed to stable biocidal isothiazolone compositions in which (1) water is substantially eliminated, (2) salt neutralization is eliminated and (3) the need for nitrate stabilizer salts is substantially eliminated.
  • orthoesters of this invention are those having the following general formula:
  • X is hydrogen, alkyl, for example alkyl of from 1 to 18 carbon atoms, or a substituted oxy of the formula OR 2 wherein R 2 is as defined below, or aryl, for example, mononuclear aryl such as phenyl and the like.
  • R 2 , R 3 and R 4 are the same or different radical selected from alkyl, for example, alkyl of from 1 to 18 carbon atoms such as methyl, ethyl, propyl, butyl, octyl and the like, and, preferably, lower (C 1 -C 5 )alkyl, cycloalkyl, for example, cycloalkyl of from 3 to 7 nuclear carbon atoms such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and the like, aryl, for example, mononuclear aryl of from 6 to 10 carbon atoms such as phenyl and the like, alkylaryl, for example lower alkyl (C 1 -C 6 ) substituted mononuclear aryl such as methylphenyl, dimethylphenyl and the like; or arylalkyl for example, mononuclear arylalkyl
  • the preferred orthoesters of this invention are those wherein R 2 , R 3 and R 4 are all lower (C 1 -C 5 )alkyl and X is hydrogen, lower (C 1 -C 5 )alkyl or aryl.
  • Especially preferred are trimethyl orthoformate, triethyl orthoformate, triethyl orthoacetate, trimethyl orthovalerate, and trimethyl orthobenzoate.
  • This invention comprises a composition which contains from about 0.1 to about 99.9 parts of one or more isothiazolones and an effective amount of an orthoester of Formula II (supra), preferably, an orthoester in the range of from 0.1 to about 99.9 percent.
  • the composition comprises at least one isothiazolone wherein Y is C 1 -C 18 alkyl or C 3 -C 12 cycloalkyl; R is hydrogen or halo; and R 1 is hydrogen or halo.
  • Typical formulation ranges are illustrated in the following Table (all percentages are parts by weight) for both a concentrated solution of the isothiazolone and a dilute solution. For certain uses, such as shipping of large quantities, more concentrated solutions may also be utilized.
  • the amount of stabilizer or mixture of stabilizers employed will be from about 1 percent to about 25 percent.
  • the isothiazolone may be present in a bulk form or packaged or encapsulated in some manner, including a form for controlled release.
  • the ratio of orthoester to isothiazolone is preferably from about 1:7 to about 1.5:1.
  • Solvents other than orthoesters may be used to dissolve the isothiazolones and may be any organic solvent which dissolves the isothiazolones, are compatable with the proposed end use, do not destabilize the isothiazolone, and do not react with the orthoester to eliminate its stabilizing action.
  • Hydroxylic solvents for example, polyols, such as glycols, alcohols and the like, may be used. Under conditions of high dilution and high ratios of stabilizer to isothiazolone, glycols may be successfully used.
  • Preferred solvents are capped polyols, wherein the free hydroxy is replaced with an ether or ester function.
  • Especially preferred are 2,5,8,11-tetraoxadecane, commonly known as triethylene glycol dimethyl ether, and 4,7-dioxaundecanol-1 acetate, commonly known as diethylene glycol butyl ether acetate.
  • the amounts of orthoester employed will vary depending on use conditions and concentrations of the isothiazolone in the mixture. In more concentrated solutions, effective amounts of orthoester based on isothiazolone are in the ratios of from about 1:4 to about 1:2. Obviously higher amounts may be used, but at additional cost. At low levels of dilution of the isothiazolone (such as from 1 to 2 percent isothiazolone in the solvent), the ratio of stabilizer to isothiazolone can range from about 1:7 to about 2:1.
  • This invention permits the stabilization of isothiazolones wherein the previously necessary stabilization salts are substantially reduced and even eliminated.
  • Useful stabilization salts which can be employed are those disclosed in U.S. Pat. Nos. 3,870,795 and 4,067,878 and include stabilization salts selected from:
  • Metal nitrates where the metal is barium, cadmium, calcium, chromium, cobalt, copper, iron, lead, lithium, magnesium, manganese, mercury, nickel, sodium, silver, strontium, tin, zinc and the like; and
  • loci are typically at any locus subject to contamination by bacteria, fungi or algae.
  • loci are in aqueous systems such as water cooling, laundry wash water, oil systems such as cutting oils, oil fields and the like where microorganisms need to be killed or where their growth needs to be controlled.
  • the stabilized biocide compositions of this invention are advantageous over salt stabilized isothiazolones described in the art and are the biocides of choice where salts pose a problem. For example, certain emulsions upon the addition of a salt may coagulate.
  • the compositions of this invention avoid this problem and therefore can be used in emulsions such as photographic emulsions, coating emulsions, (e.g. paints) to form solid protective or decorative films; electronic circuitry, wood, metals, plastics, fibers, membranes, carpet backings, ceramics and the like where surfaces need to be coated or protected, adhesives, caulks, and sensitive emulsions.
  • compositions of this invention are useful in fuel systems such as diesel fuel, gasoline, kerosene, certain alcohols, and the like, because they eliminate the possibility of salt deposits on component parts. Another reason for eliminating salts is to avoid an environment in which corrosion can occur. For example, chloride salts (among others) have a corrosive effect on many metals and are to be avoided where possible.
  • isothiazolone stabilizers of this invention have other applications known to those skilled in the art.
  • orthoformates are known to serve as reactive scavengers for molecules containing --OH, --NH 2 , --SH and other nucleophilic groups.
  • a biocide formulation stabilized with an orthoformate would be particularly advantageous where the dual function of biocidal/biostatic activity and scavenging would lead to advantageous results.
  • salts in the isothiazolones as salts may contribute to deterioration of optical properties and/or increase water pickup and haze levels.
  • nitrate salts avoids the possibility of nitrosamine formation with any amines present in the formulation. Removal of multivalent cations from the biocide may also eliminate the known possibility of creating physical incompatibility problems in certain cosmetic formulations caused by precipitation of salts or complexes.
  • biocides can frequently be enhanced by combination with one or more other biocides.
  • biocides there have been numerous examples of synergistic combinations of biocides.
  • other known biocides may be combined advantageously with the stabilized isothiazolones of this invention.
  • Isothiazolones are used as disinfectants, in oil field water treatment, as watercooling system microbiocides, as preservatives for aqueous dispersions or organic polymers, as wood pulp white water slimicides, as cosmetic preservatives, as cutting oil, jet fuel, and heating oil preservatives, and the like. Solutions of isothiazolones are also applied to a solid substrate, such as fabric, leather, or wood, as a preservative, or admixed with plastics.
  • the products of this invention are especially useful as preservatives for the following:
  • Emulsions and dispersions that are sensitive to divalent cations are those contained in a wide variety of products, such as paints, cosmetics, floor polishes and binders
  • Plastics as it eliminates or substantially reduces precipitated salts which can contribute directly or indirectly to haze, opacity, or physical weakness in the surface.
  • orthoester is well-known in the field of organic chemistry. They can also be named as ethers. Thus triethyl orthoacetate is named 1,1,1-trimethoxyethane, trimethyl orthobenzoate is tris(methoxy)methylbenzene.
  • the orthoesters (1A) of this invention are known compounds or may be prepared by methods well known to those skilled in the art.
  • Orthocarbonate esters may be prepared by a related method ##STR3##
  • Mixed orthoesters, (R 2 ⁇ R 3 ) may be prepared from the iminoether hydrochloride of the parent acid as illustrated by the following equations: ##STR4##
  • Derivatives of benzoic acid and related aromatic acids may be prepared by similar chemistry or by a controlled Grignard reaction on an orthocarbonate.
  • the 3:1 mixture of 5-chloro-2-methylisothiazolin-3-one/2-methylisothiazolin-3-one (16.2%) is mixed at 14% active ingredient (AI) in triglyme (76.8%) with the chosen stabilizer (7%).
  • AI active ingredient
  • HPLC HPLC is used to measure of AI. Maintenance of AI must be >85% to meet the target of most preferred. Other stabilizers may be less effective in the test, but may be adequate for stabilization under shorter time, less exacerbated conditions. This is compared with a 3:1 mixture of 5-cloro-2-methylisothiazolin-3-one/2-methylisothiazolin-3-one stabilized with magnesium nitrate (15%).
  • a solution containing 1.5% of N-methyl-5-chloroisothiazolin-3-one and N-methylisothiazolin-3-one, and 2.0% of triethyl orthoformate as stabilizer in 96.5 dipropylene glycol is used as a preservative for a hair shampoo.
  • Salt shock is observed as a precipitate or gelatinous mass that forms in the polymer emulsion when isothiazolone, containing stabilizers composed of divalent metal ions (e.g. Mg ++ , Cu ++ ), is added as a preservative.
  • divalent metal ions e.g. Mg ++ , Cu ++
  • the polymer emulsion is initially passed through a 325 mesh screen to remove any gel that might be present from manufacture. Isothiazolone is added to a total amount of 30 ppm AI based on total polymer emulsion A 250 g. emulsion sample in a pint container is used. The sample is gently swirled after pipetting the appropriate amount of isothiazolone. The sample is inverted twice to mix and allowed to stand at ambient temperature for sixty minutes. The sample is again passed through a 325 mesh screen Any gel or precipitate on the screen is washed with deionized water to remove residual, uncoagulated polymer emulsion. The material remaining on the screen is collected and dried overnight at 50° C. This is followed by heating 1 hour at 150° C. to remove any remaining water. The residue is then weighed.
  • the small amount of gel formed when the emulsion is preserved with stabilized isothiazolone ( ⁇ 60 mg/kg emulsion) will not be detrimental in the use of the emulsion in various applications such as paints, caulks, and the like.
  • the amount of gel formed (>2400 mg/kg emulsion) when salt stabilized isothiazolone is used as a preservative would be easily visible and objectionable.
  • This test measures bactericidal activity in water free of organic matter It measures the loss of cell viability in an aqueous suspension of bacterial cells as a function of time when these cells are contacted with a defined concentration of test compound in the water. This is done by taking aliquots of the cell suspensions at the appropriate time interval and assaying the number of viable cells per milliliter by plate count or most probably number (MPN) methodology. These measurements are done on the cell suspensions containing no test compound. The viable cell counts of the test and control samples are then compared to determine cell death.
  • MPN most probably number
  • the inoculum is prepared by growing the bacteria on a slant for 24 hours and then harvesting the cells into phosphate buffer. To start the test at zero time, one volume of bacterial inoculum is added to 100 volumes of test solution containing compound at the final test concentration.
  • results are calculated in terms of log10 reduction in MPN/ml compared to aqueous control This is done by taking the logarithm base 10 of the MPN/ml for the test count and subtracting this number from the logarithm base 10 of the MPN/ml for the aqueous control count.
  • One log reduction corresponds to 90% kill
  • 2 logs reduction corresponds to 99% kill
  • 3 logs reduction corresponds to 99.9% kill, etc.
  • MIC minimum inhibitory concentration
  • a minimum inhibitory concentration (MIC) test is used to evaluate the antimicrobial activity of a test compound in preservative applications.
  • the MIC value is obtained in the following manner. A volume of the stock solution containing 1% AI is dispensed into enrichment broth to give an initial starting test concentration of 250 ppm compound.
  • each vessel in the dilution series contains an equal volume of the compound free broth.
  • the first vessel contains twice the volume of broth with the starting concentration of test compound.
  • One-half of the broth from the first vessel is transferred to the second vessel.
  • one-half the resulting volume is removed from the second vessel and transferred to the third vessel.
  • the entire cycle is repeated 8 to 12 times, depending on the number of dilutions desired. The result is a two-fold serial dilution of test compound in the enrichment broth.
  • Each vessel is then inoculated with a cell suspension of the appropriate test organism.
  • Bacteria are grown in broth and fungi on agar slants, for a time and at a temperature appropriate to the species being tested. At the end of the growth period, the broth is vortexed to disperse the cells.
  • the spores are harvested by pipetting water onto the slant and dislodging the spores with a sterile loop
  • the cell/spore suspensions are standardized by controlling incubation time and temperature and the volume of the diluent.
  • the vessels are incubated at the appropriate temperature, and then examined for growth/no growth.
  • the minimum inhibitory concentration (MIC) is defined as the lowest concentration of compound that results in complete inhibition of growth of the test organism.

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Toxicology (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Steroid Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Dental Preparations (AREA)
  • Paints Or Removers (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Cosmetics (AREA)
  • Polymerisation Methods In General (AREA)
US07/118,366 1987-11-06 1987-11-06 Organic stabilizers Expired - Lifetime US4906274A (en)

Priority Applications (22)

Application Number Priority Date Filing Date Title
US07/118,366 US4906274A (en) 1987-11-06 1987-11-06 Organic stabilizers
CA000580959A CA1301061C (en) 1987-11-06 1988-10-21 Orthoester stabilizers for 3-isothiazolones
IE331088A IE62806B1 (en) 1987-11-06 1988-11-02 Stabilized isothiazolone compositions
NO884873A NO174991C (no) 1987-11-06 1988-11-02 Stabilt isotiazolonpreparat og anvendelse derav
HU885697A HU202053B (en) 1987-11-06 1988-11-03 Stabilized isothiazolon compositions
MX13658A MX164009B (es) 1987-11-06 1988-11-03 Estabilizadores organicos
MYPI88001255A MY103633A (en) 1987-11-06 1988-11-03 Stabilized isothiazolone compositions
DK618388A DK618388A (da) 1987-11-06 1988-11-04 Stabiliserede isothiazolonpraeparater
FI885110A FI89855C (fi) 1987-11-06 1988-11-04 Stabiliserade isotiazolonkompositioner
BR888805762A BR8805762A (pt) 1987-11-06 1988-11-04 Composicoes estaveis,a base de 3-isotiazolonas
AU24718/88A AU609204B2 (en) 1987-11-06 1988-11-04 Stabilized isothiazolone compositions
DE8888310390T DE3877899T2 (de) 1987-11-06 1988-11-04 Stabilisierte isothiazolon-zusammensetzungen.
IL88292A IL88292A (en) 1987-11-06 1988-11-04 Stabilized biocidal isothiazolone compositions
ES88310390T ES2053763T3 (es) 1987-11-06 1988-11-04 Composiciones estabilizadas de isotiazolonas.
EP88310390A EP0315464B1 (de) 1987-11-06 1988-11-04 Stabilisierte Isothiazolon-Zusammensetzungen
AT88310390T ATE85053T1 (de) 1987-11-06 1988-11-04 Stabilisierte isothiazolon-zusammensetzungen.
NZ226846A NZ226846A (en) 1987-11-06 1988-11-04 Compositions of biocidal isothiazolone derivatives containing orthoester stabiliser
JP63279203A JPH0818932B2 (ja) 1987-11-06 1988-11-04 安定化されたイソチアゾロン組成物
KR1019880014594A KR970007930B1 (ko) 1987-11-06 1988-11-07 유기 안정제
PH37825A PH24910A (en) 1987-11-06 1988-11-17 Organic stabilizers
GR920403281T GR3006903T3 (de) 1987-11-06 1993-01-28
SG300/93A SG30093G (en) 1987-11-06 1993-03-18 Stabilized isothiazolone compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US07/118,366 US4906274A (en) 1987-11-06 1987-11-06 Organic stabilizers

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US4906274A true US4906274A (en) 1990-03-06

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US07/118,366 Expired - Lifetime US4906274A (en) 1987-11-06 1987-11-06 Organic stabilizers

Country Status (22)

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US (1) US4906274A (de)
EP (1) EP0315464B1 (de)
JP (1) JPH0818932B2 (de)
KR (1) KR970007930B1 (de)
AT (1) ATE85053T1 (de)
AU (1) AU609204B2 (de)
BR (1) BR8805762A (de)
CA (1) CA1301061C (de)
DE (1) DE3877899T2 (de)
DK (1) DK618388A (de)
ES (1) ES2053763T3 (de)
FI (1) FI89855C (de)
GR (1) GR3006903T3 (de)
HU (1) HU202053B (de)
IE (1) IE62806B1 (de)
IL (1) IL88292A (de)
MX (1) MX164009B (de)
MY (1) MY103633A (de)
NO (1) NO174991C (de)
NZ (1) NZ226846A (de)
PH (1) PH24910A (de)
SG (1) SG30093G (de)

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5118699A (en) * 1990-12-10 1992-06-02 Rohm And Haas Company Use of hydrazide stabilizers for 3-isothiazolones
US5127934A (en) * 1988-05-16 1992-07-07 Rohm And Haas Company Stabilized compositions comprising isothiazolones and epoxides
US5142058A (en) * 1990-12-14 1992-08-25 Rohm And Haas Company Halogen-containing organic stabilizers for 3-isothiazolones
US5145981A (en) * 1990-12-10 1992-09-08 Rohm And Haas Use of antimony salt stabilizers for 3-isothiazolones
US5145501A (en) * 1991-11-12 1992-09-08 Rohm And Haas Company Bromate stabilizers for 3-isothiazolones
US5342836A (en) * 1992-08-11 1994-08-30 Rohm And Haas Company Nitrogen-based stabilizers for 3-isothiazolones
US5373016A (en) * 1993-05-28 1994-12-13 Zeneca, Inc. Protection of isothiazolinone biocides from free radicals
EP0686347A2 (de) 1994-06-08 1995-12-13 Rohm And Haas Company Zusammensetzung enthaltend 3-Isothiazolen und Stabilisator
EP0686346A1 (de) 1994-06-06 1995-12-13 Rohm And Haas Company Zusammensetzung, die 3-Isothiazolone und Stabilisatoren enthält
US5534487A (en) * 1995-05-16 1996-07-09 Rohm And Haas Company Stabilization of 3-isothiazolone solutions
US5594017A (en) * 1995-05-25 1997-01-14 Rohm And Haas Company Stabilization of aqueous 3-isothiazolone solutions
US5668083A (en) * 1995-06-06 1997-09-16 Rohm And Haas Company Composition containing 3-isothiazolone and stabilizer
US6135121A (en) * 1996-06-28 2000-10-24 Regent Court Technologies Tobacco products having reduced nitrosamine content
US6202649B1 (en) 1996-12-02 2001-03-20 Regent Court Technologies Method of treating tobacco to reduce nitrosamine content, and products produced thereby
US20010000386A1 (en) * 1999-04-26 2001-04-26 Peele David Mccray Tobacco processing
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DE102004052878A1 (de) 2004-11-02 2006-05-04 Schülke & Mayr GmbH Isothiazolonhaltige Konservierungsmittel mit verbesserter Stabilität

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US5127934A (en) * 1988-05-16 1992-07-07 Rohm And Haas Company Stabilized compositions comprising isothiazolones and epoxides
US5118699A (en) * 1990-12-10 1992-06-02 Rohm And Haas Company Use of hydrazide stabilizers for 3-isothiazolones
US5145981A (en) * 1990-12-10 1992-09-08 Rohm And Haas Use of antimony salt stabilizers for 3-isothiazolones
US5142058A (en) * 1990-12-14 1992-08-25 Rohm And Haas Company Halogen-containing organic stabilizers for 3-isothiazolones
US5145501A (en) * 1991-11-12 1992-09-08 Rohm And Haas Company Bromate stabilizers for 3-isothiazolones
US5342836A (en) * 1992-08-11 1994-08-30 Rohm And Haas Company Nitrogen-based stabilizers for 3-isothiazolones
US5373016A (en) * 1993-05-28 1994-12-13 Zeneca, Inc. Protection of isothiazolinone biocides from free radicals
EP0686346A1 (de) 1994-06-06 1995-12-13 Rohm And Haas Company Zusammensetzung, die 3-Isothiazolone und Stabilisatoren enthält
EP0686347A2 (de) 1994-06-08 1995-12-13 Rohm And Haas Company Zusammensetzung enthaltend 3-Isothiazolen und Stabilisator
US5534487A (en) * 1995-05-16 1996-07-09 Rohm And Haas Company Stabilization of 3-isothiazolone solutions
US5594017A (en) * 1995-05-25 1997-01-14 Rohm And Haas Company Stabilization of aqueous 3-isothiazolone solutions
US5668083A (en) * 1995-06-06 1997-09-16 Rohm And Haas Company Composition containing 3-isothiazolone and stabilizer
USRE38123E1 (en) 1996-06-28 2003-05-27 Regent Court Technologies, Llc. Tobacco products having reduced nitrosamine content
US6311695B1 (en) 1996-06-28 2001-11-06 Regent Court Technologies Method of treating tobacco to reduce nitrosamine content, and products produced thereby
US6338348B1 (en) 1996-06-28 2002-01-15 Regent Court Technologies Method of treating tobacco to reduce nitrosamine content, and products produced thereby
US6135121A (en) * 1996-06-28 2000-10-24 Regent Court Technologies Tobacco products having reduced nitrosamine content
US6425401B1 (en) 1996-12-02 2002-07-30 Regent Court Technologies Llc Method of treating tobacco to reduce nitrosamine content, and products produced thereby
US20020174874A1 (en) * 1996-12-02 2002-11-28 Regent Court Technologies Llc Method of treating tobacco to reduce nitrosamine content, and products produced thereby
US6202649B1 (en) 1996-12-02 2001-03-20 Regent Court Technologies Method of treating tobacco to reduce nitrosamine content, and products produced thereby
US6895974B2 (en) 1999-04-26 2005-05-24 R. J. Reynolds Tobacco Company Tobacco processing
US20010000386A1 (en) * 1999-04-26 2001-04-26 Peele David Mccray Tobacco processing
US20030047190A1 (en) * 1999-04-26 2003-03-13 Peele David Mccray Tobacco processing
US7404406B2 (en) 1999-04-26 2008-07-29 R. J. Reynolds Tobacco Company Tobacco processing
US6805134B2 (en) 1999-04-26 2004-10-19 R. J. Reynolds Tobacco Company Tobacco processing
US20050022832A1 (en) * 1999-04-26 2005-02-03 Peele David Mccray Tobacco processing
US6514299B1 (en) 2000-11-09 2003-02-04 Millennium Fuels Usa, Llc Fuel additive and method therefor
US20040101539A1 (en) * 2002-11-22 2004-05-27 Ernst Engler Aqueous dispersion of low-melting organic solids
US8151804B2 (en) 2008-12-23 2012-04-10 Williams Jonnie R Tobacco curing method

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FI89855B (fi) 1993-08-31
GR3006903T3 (de) 1993-06-30
IE883310L (en) 1989-05-06
MY103633A (en) 1993-08-28
NO174991B (no) 1994-05-09
FI89855C (fi) 1993-12-10
EP0315464B1 (de) 1993-01-27
AU609204B2 (en) 1991-04-26
DK618388D0 (da) 1988-11-04
EP0315464A1 (de) 1989-05-10
NO174991C (no) 1994-08-17
DE3877899T2 (de) 1993-06-09
JPH0818932B2 (ja) 1996-02-28
DE3877899D1 (de) 1993-03-11
FI885110A (fi) 1989-05-07
IL88292A (en) 1992-11-15
HUT49784A (en) 1989-11-28
NZ226846A (en) 1991-09-25
AU2471888A (en) 1989-05-11
IL88292A0 (en) 1989-06-30
IE62806B1 (en) 1995-03-08
NO884873D0 (no) 1988-11-02
KR970007930B1 (ko) 1997-05-19
SG30093G (en) 1993-06-25
JPH01157971A (ja) 1989-06-21
ATE85053T1 (de) 1993-02-15
ES2053763T3 (es) 1994-08-01
KR890007638A (ko) 1989-07-05
NO884873L (no) 1989-05-08
FI885110A0 (fi) 1988-11-04
CA1301061C (en) 1992-05-19
BR8805762A (pt) 1989-07-25
PH24910A (en) 1990-12-26
MX164009B (es) 1992-07-09
HU202053B (en) 1991-02-28
DK618388A (da) 1989-05-07

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